Zobrazeno 1 - 10
of 168
pro vyhledávání: '"Algirdas, Utkus"'
Autor:
Robertas Strumila, Aiste Lengvenyte, Linas Zdanavicius, Robertas Badaras, Edgaras Dlugauskas, Sigita Lesinskiene, Eimantas Matiekus, Martynas Marcinkevicius, Lina Venceviciene, Algirdas Utkus, Andrius Kaminskas, Tomas Petrenas, Jurgita Songailiene, Dalius Vitkus, Laima Ambrozaityte
Publikováno v:
Comprehensive Psychoneuroendocrinology, Vol 19, Iss , Pp 100235- (2024)
Introduction: Suicidal ideation, an important risk factor for suicide attempts, has an unclear neurobiological basis and is potentially linked to the dysregulation of the hypothalamic-pituitary-adrenal (HPA) axis and immune-inflammatory systems. Whil
Externí odkaz:
https://doaj.org/article/6dc41990830b4ea2923ae25e33e1720a
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background Mitochondrial Diseases (MDs) are a diverse group of neurometabolic disorders characterized by impaired mitochondrial oxidative phosphorylation and caused by pathogenic variants in more than 400 genes. The implementation of next-ge
Externí odkaz:
https://doaj.org/article/78143742ef154dcc97f3618a8d1aa48b
Autor:
Min-Yu Lan, Tsu-Kung Lin, Baiba Lace, Algirdas Utkus, Birute Burnyte, Kristina Grigalioniene, Yu-Han Lin, Inna Inashkina, Chia-Wei Liou
Publikováno v:
Cells, Vol 13, Iss 8, p 694 (2024)
Variants of mitochondrial DNA (mtDNA) have been identified as risk factors for the development of Parkinson’s disease (PD). However, the underlying pathogenetic mechanisms remain unclear. Cybrid models carrying various genotypes of mtDNA variants w
Externí odkaz:
https://doaj.org/article/cc2baf2bc8854905bc64071550759ef6
Autor:
Gryko, Mariusz, Łukaszewicz-Zając, Marta, Guzińska-Ustymowicz, Katarzyna, Kucharewicz, Mariola, Mroczko, Barbara, Algirdas, Utkus
Publikováno v:
In Advances in Medical Sciences March 2023 68(1):94-100
Autor:
Birute Tumiene, Harm Peters, Bela Melegh, Borut Peterlin, Algirdas Utkus, Natalja Fatkulina, György Pfliegler, Holm Graessner, Sanja Hermanns, Maurizio Scarpa, Jean-Yves Blay, Sharon Ashton, Lucy McKay, Gareth Baynam
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-20 (2022)
Abstract People living with rare diseases (PLWRD) still face huge unmet needs, in part due to the fact that care systems are not sufficiently aligned with their needs and healthcare workforce (HWF) along their care pathways lacks competencies to effi
Externí odkaz:
https://doaj.org/article/6407632929da40bb8a36b39315418770
Autor:
Matilde Malcorps, Silvia Amor-Barris, Birute Burnyte, Ramune Vilimiene, Camila Armirola-Ricaurte, Kristina Grigalioniene, Alexandra Ekshteyn, Ausra Morkuniene, Arunas Vaitkevicius, Els De Vriendt, Jonathan Baets, Steven S. Scherer, Laima Ambrozaityte, Algirdas Utkus, Albena Jordanova, Kristien Peeters
Publikováno v:
Orphanet Journal of Rare Diseases, Vol 17, Iss 1, Pp 1-11 (2022)
Abstract Background Recessive loss-of-function variations in HINT1 cause a peculiar subtype of Charcot-Marie-Tooth disease: neuromyotonia and axonal neuropathy (NMAN; OMIM[#137200]). With 25 causal variants identified worldwide, HINT1 mutations are a
Externí odkaz:
https://doaj.org/article/b4607f9f7eb949f7be4eff8b58b7b82a
Autor:
Eglė Mazgelytė, Agnė Valatkevičiūtė, Jurgita Songailienė, Algirdas Utkus, Neringa Burokienė, Dovilė Karčiauskaitė
Publikováno v:
Frontiers in Endocrinology, Vol 14 (2023)
BackgroundPoor sleep quality is associated with different physical and mental health diseases. It is proposed that increased hypothalamic-pituitary-adrenal axis activity is a potential contributor affecting sleep pattern and quality. We aimed to anal
Externí odkaz:
https://doaj.org/article/3ac1177d628245369b4ae1cf87f32452
Autor:
Sigita Lesinskienė, Emilijus Žilinskas, Algirdas Utkus, Rūta Marčiukaitytė, Gabrielė Vasiliauskaitė, Rugilė Stankevičiūtė, Odeta Kinčinienė
Publikováno v:
Children, Vol 11, Iss 1, p 5 (2023)
Prenatal alcohol exposure is one of the major avoidable causes of developmental disruption and health abnormalities in children. Fetal alcohol spectrum disorders (FASDs), a significant consequence of prenatal alcohol exposure, have gained more attent
Externí odkaz:
https://doaj.org/article/8ca8a0795a094c5e85b24ec296f70291
Autor:
Kristina Grigalionienė, Birutė Burnytė, Danutė Balkelienė, Laima Ambrozaitytė, Algirdas Utkus
Publikováno v:
Molecular Genetics & Genomic Medicine, Vol 11, Iss 1, Pp n/a-n/a (2023)
Abstract Background Kearns‐Sayre syndrome (KSS) is a rare multisystem mitochondrial disorder characterized by onset before 20 years of age and a typical clinical triad: progressive external ophthalmoplegia, pigmentary retinopathy and cardiac conduc
Externí odkaz:
https://doaj.org/article/5b144b7492a24501b535e885d1c7a127
Autor:
Evelina Siavrienė, Gunda Petraitytė, Birutė Burnytė, Aušra Morkūnienė, Violeta Mikštienė, Tautvydas Rančelis, Algirdas Utkus, Vaidutis Kučinskas, Eglė Preikšaitienė
Publikováno v:
BMC Musculoskeletal Disorders, Vol 22, Iss 1, Pp 1-8 (2021)
Abstract Background Autosomal recessive limb–girdle muscular dystrophy-1 (LGMDR1), also known as calpainopathy, is a genetically heterogeneous disorder characterised by progression of muscle weakness. Homozygous or compound heterozygous variants in
Externí odkaz:
https://doaj.org/article/9fa109b82e7f4d818b1ad473453435d8